Symbol Name ID |
Epb41l1
erythrocyte membrane protein band 4.1 like 1 MGI:103010 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Atypical behavior |
Disease(s) Associated with EPB41L1 | ||
autosomal dominant intellectual developmental disorder 11 |
Mouse Phenotypes | increased exploration in new environment |
decreased thigmotaxis |
increased startle reflex |
decreased grip strength |
abnormal locomotor behavior |
hyperactivity |
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Availability | Mouse Genotype | ||||||
Epb41l1tm1b(EUCOMM)Wtsi/Epb41l1tm1b(EUCOMM)Wtsi |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 09/03/2024 MGI 6.24 |
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